Device recall
Z-0986-04: MinXray P200R40 Mobile Podiatry X-Ray System, Model PM200R40 (mobile) and…
FDA device recall · Class II · Minxray Inc
Key facts
| Recall number (Z-number) | Z-0986-04 |
|---|---|
| Recall event | 29354 |
| Product | MinXray P200R40 Mobile Podiatry X-Ray System, Model PM200R40 (mobile) and PW200R40 (wall mounted), MinXray, Inc., 3611 Commercial Avenue, Northbrook, Illinois 60062-1822 U.S.A. |
| Product code | DS-21 |
| Recalling firm | Minxray Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2005 |
| FEI number | 1418960 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database